Skip to content

A study comparing different techniques of reducing surgery related anxiety among children

A randomized controlled trial on non-pharmacological techniques of reducing anxiety among children undergoing elective surgeries - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104278
Enrollment
120
Registered
2026-02-19
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Control group: The anaesthetist verbally informs and consoles the patient, inside the OR before surgery- according to his/ her own discretion Control Intervention1: Cartoon video group:
each having 3-5 minutes duration Control Intervention2: Virtual Reality tour of Operation theatre- group: Smartphone compatible virtual reality headset (VR Boxâ?¢) (40 mm lens in 3D box with head-stra

Sponsors

Department of Anaesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA grade: I, II 2. Patients who are scheduled for any elective diagnostic or therapeutic surgical procedure 3. Patients whose parent/ LAR are willing to give written consent

Exclusion criteria

Exclusion criteria: 1.Patient refusal at any stage, even after parent/LAR have given consent 2. ASA grade III/ IV/V 3. Patients who are expected to be sedated/ mechanically ventilated or shifted to ICU after surgery 4. Patients who have undergone surgery/or anaesthesia in the past 5. Any psychological/ behavioral disorder, those on psychoactive medications, those with history of epilepsy or seizure 6. Blind, deaf and mute patients

Design outcomes

Primary

MeasureTime frame
modified Yale Preoperative Anxiety score reduction from baseline, to post interventionTimepoint: Baseline- in the preanaesthesia room, Post intervention- immediately after shifting inside OR before induction of anaesthesia; and third reading- immediately after recovery in the recovery room

Secondary

MeasureTime frame
Studying the acceptance rate of the different anxiolysis techniques among the study participantsTimepoint: Baseline- only once while introducing the intervention first time, to each patient

Countries

India

Contacts

Public ContactSreyashi Naskar

Indira Gandhi Institute of Child Health, Bangalore

sreyashi.n@gmail.com6290153836

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026